Mitochondrial genomes revisited: why do different lineages retain different genes?
BMC Biology,
Journal Year:
2024,
Volume and Issue:
22(1)
Published: Jan. 25, 2024
Abstract
The
mitochondria
contain
their
own
genome
derived
from
an
alphaproteobacterial
endosymbiont.
From
thousands
of
protein-coding
genes
originally
encoded
by
ancestor,
only
between
1
and
about
70
are
on
extant
mitochondrial
genomes
(mitogenomes).
Thanks
to
a
dramatically
increasing
number
sequenced
annotated
mitogenomes
coherent
picture
why
some
were
lost,
or
relocated
the
nucleus,
is
emerging.
In
this
review,
we
describe
characteristics
mitochondria-to-nucleus
gene
transfer
resulting
varied
content
across
eukaryotes.
We
introduce
‘burst-upon-drift’
model
best
explain
nuclear-mitochondrial
population
genetics
with
flares
due
genetic
drift.
Language: Английский
Is the Mutation Rate Lower in Genomic Regions of Stronger Selective Constraints?
Molecular Biology and Evolution,
Journal Year:
2022,
Volume and Issue:
39(8)
Published: July 30, 2022
Abstract
A
study
of
the
plant
Arabidopsis
thaliana
detected
lower
mutation
rates
in
genomic
regions
where
mutations
are
more
likely
to
be
deleterious,
challenging
principle
that
mutagenesis
is
blind
its
consequence.
To
examine
generality
this
finding,
we
analyze
large
mutational
data
from
baker's
yeast
and
humans.
The
do
not
exhibit
trend,
whereas
human
show
an
opposite
trend
disappears
upon
control
potential
confounders.
We
find
identified
substantially
than
reported
original
data-generating
studies
expected
Arabidopsis'
rate.
These
extra
enriched
polynucleotide
tracts
have
relatively
low
sequencing
qualities
so
errors.
Furthermore,
“mutations”
can
produce
purported
Arabidopsis.
Together,
our
results
support
stronger
selective
constraints
plant,
fungal,
animal
models
examined.
Language: Английский
DNA fun facts: Hypermutable DNA, mutagenic DNA break repair, and transcription-associated mutagenesis
Elsevier eBooks,
Journal Year:
2025,
Volume and Issue:
unknown, P. 31 - 78
Published: Jan. 1, 2025
Language: Английский
Spontaneous and environment induced genomic alterations in yeast model
Kejing Li,
No information about this author
Lei S. Qi,
No information about this author
Ying-Xuan Zhu
No information about this author
et al.
Cell Insight,
Journal Year:
2024,
Volume and Issue:
4(1), P. 100209 - 100209
Published: Sept. 26, 2024
Language: Английский
Mutations in yeast are deleterious on average regardless of the degree of adaptation to the testing environment
Kevin Bao,
No information about this author
Brant R. Strayer,
No information about this author
Neil P. Braker
No information about this author
et al.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Jan. 11, 2024
Abstract
The
role
of
spontaneous
mutations
in
evolution
depends
on
the
distribution
their
effects
fitness.
Despite
a
general
consensus
that
new
are
deleterious
average,
handful
mutation
accumulation
experiments
diverse
organisms
instead
suggest
beneficial
and
can
have
comparable
fitness
impacts,
i.e.,
product
respective
rates
be
roughly
equal.
We
currently
lack
framework
for
predicting
when
such
pattern
will
occur.
One
idea
is
more
evident
genotypes
not
well
adapted
to
testing
environment.
tested
this
prediction
experimentally
laboratory
yeast
Saccharomyces
cerevisiae
by
allowing
nine
replicate
populations
adapt
novel
environments
with
complex
sets
stressors.
After
>1000
asexual
generations
interspersed
41
rounds
sexual
reproduction,
we
assessed
mean
effect
induced
growth
both
environment
which
they
had
been
adapting
alternative
were
severity
depending
However,
find
no
evidence
adaptive
match
between
genotype
predictive
mutational
effects.
Language: Английский
Spontaneous single-nucleotide substitutions and microsatellite mutations have distinct distributions of fitness effects
PLoS Biology,
Journal Year:
2024,
Volume and Issue:
22(7), P. e3002698 - e3002698
Published: July 1, 2024
The
fitness
effects
of
new
mutations
determine
key
properties
evolutionary
processes.
Beneficial
drive
evolution,
yet
selection
is
also
shaped
by
the
frequency
small-effect
deleterious
mutations,
whose
combined
effect
can
burden
otherwise
adaptive
lineages
and
alter
trajectories
outcomes
in
clonally
evolving
organisms
such
as
viruses,
microbes,
tumors.
small
sizes
these
important
have
made
accurate
measurements
their
rates
difficult.
In
assessing
on
growth
be
especially
instructive,
this
complex
phenotype
closely
linked
to
organisms.
Here,
we
perform
high-throughput
time-lapse
microscopy
cells
from
mutation-accumulation
strains
precisely
infer
distribution
mutational
rate
budding
yeast,
Saccharomyces
cerevisiae
.
We
show
that
are
overwhelmingly
negative,
highly
skewed
towards
very
sizes,
frequent
enough
suggest
hitchhikers
may
impose
a
significant
lineages.
By
using
lines
accumulated
either
wild-type
or
slippage
repair-defective
backgrounds,
further
disentangle
2
common
types
single-nucleotide
substitutions
simple
sequence
repeat
indels,
they
distinct
yeast
rate.
Although
average
mutation
(approximately
0.3%),
many
do
rate,
implying
class
has
an
impact.
Language: Английский
Two independent DNA repair pathways cause mutagenesis in template switching deficientSaccharomyces cerevisiae
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2023,
Volume and Issue:
unknown
Published: June 26, 2023
Abstract
Upon
DNA
replication
stress,
cells
utilize
the
post-replication
repair
pathway
to
single-stranded
and
maintain
genome
integrity.
Post-replication
is
divided
into
two
branches:
error-prone
translesion
synthesis,
signaled
by
PCNA
mono-ubiquitination,
error-free
template
switching,
poly-ubiquitination.
In
Saccharomyces
cerevisiae
,
Rad5
involved
in
both
branches
of
during
stress.
When
poly-ubiquitination
function
disrupted,
recruits
synthesis
polymerases
stalled
forks,
resulting
mutagenic
repair.
Details
how
carried
out,
as
well
relationship
between
Rad5-mediated
canonical
PCNA-mediated
repair,
remain
be
understood.
We
find
that
requires
polymerase
ζ
but
does
not
require
other
yeast
activities.
Furthermore,
we
show
independent
binding
Rev1
so
separable
from
absence
modes
contribute
additively
stress
response
a
timing-independent
manner.
Cellular
contexts
where
switching
compromised
are
simply
laboratory
phenomena,
natural
variant
RAD5
defective
therefore
Rad5-
Our
results
highlight
importance
regulating
spontaneous
mutagenesis
genetic
diversity
S.
through
different
Language: Английский
Spontaneous single-nucleotide substitutions and microsatellite mutations have distinct distributions of fitness effects
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2023,
Volume and Issue:
unknown
Published: July 4, 2023
Abstract
The
fitness
effects
of
new
mutations
determine
key
properties
evolutionary
processes.
Beneficial
drive
evolution,
yet
selection
is
also
shaped
by
the
frequency
small-effect
deleterious
mutations,
whose
combined
effect
can
burden
otherwise
adaptive
lineages
and
alter
trajectories
outcomes
in
clonally
evolving
organisms
such
as
viruses,
microbes,
tumors.
small
sizes
these
important
have
made
accurate
measurements
their
rates
difficult.
In
assessing
on
growth
be
especially
instructive,
this
complex
phenotype
closely
linked
to
organisms.
Here,
we
perform
high-throughput
time-lapse
microscopy
cells
from
mutation-accumulation
strains
precisely
infer
distribution
mutational
rate
budding
yeast,
Saccharomyces
cerevisiae
.
We
show
that
are
overwhelmingly
negative,
highly
skewed
towards
very
sizes,
frequent
enough
suggest
hitchhikers
may
impose
a
significant
lineages.
By
using
lines
accumulated
either
wild-type
or
slippage
repair-defective
backgrounds,
further
disentangle
two
common
types
single-nucleotide
substitutions
simple
sequence
repeat
indels,
they
distinct
yeast
rate.
Although
average
mutation
(∼0.3%),
many
do
rate,
implying
class
has
an
impact.
Language: Английский
Two independent DNA repair pathways cause mutagenesis in template switching deficient Saccharomyces cerevisiae
Genetics,
Journal Year:
2023,
Volume and Issue:
225(3)
Published: Aug. 18, 2023
Abstract
Upon
DNA
replication
stress,
cells
utilize
the
postreplication
repair
pathway
to
single-stranded
and
maintain
genome
integrity.
Postreplication
is
divided
into
2
branches:
error-prone
translesion
synthesis,
signaled
by
proliferating
cell
nuclear
antigen
(PCNA)
monoubiquitination,
error-free
template
switching,
PCNA
polyubiquitination.
In
Saccharomyces
cerevisiae,
Rad5
involved
in
both
branches
of
during
stress.
When
polyubiquitination
function
s
disrupted,
recruits
synthesis
polymerases
stalled
forks,
resulting
mutagenic
repair.
Details
how
carried
out,
as
well
relationship
between
Rad5-mediated
canonical
PCNA-mediated
repair,
remain
be
understood.
We
find
that
requires
polymerase
ζ
but
does
not
require
other
yeast
activities.
Furthermore,
we
show
independent
binding
Rev1
so
separable
from
absence
modes
contribute
additively
stress
response
a
timing-independent
manner.
Cellular
contexts
where
switching
compromised
are
simply
laboratory
phenomena,
natural
variant
RAD5
defective
therefore
Rad5-
Our
results
highlight
importance
regulating
spontaneous
mutagenesis
genetic
diversity
S.
cerevisiae
through
different
Language: Английский